![]() Bayer AktiengesellschaftLeverkusenInterim Report as of June 30, 2017A Interim Group Management ReportSecond quarter of 2017Bayer: Group performance matches prior year despite declines at Crop Science
Economic Position of the Bayer GroupThe Bayer Group increased sales by 1.9% (Fx & portfolio adj.) to €12.2 billion in
the second quarter of 2017. EBITDA before special items matched the prior-year period,
coming in at €3.1 billion (+ 0.1%). We achieved encouraging growth in earnings and
margins at Pharmaceuticals and Animal Health. Business declined at Consumer Health,
in particular due to the difficult market environment in the United States. Against
the backdrop of high inventories in Brazil, the world's second-largest agriculture
market, we posted substantial declines in sales and earnings at Crop Science. As such,
sales and earnings of our Life Science businesses were down. Covestro once again posted
substantial growth in sales and earnings. Key EventsOn June 7, 2017, Bayer reduced its directly held interest in Covestro from 53.3% to
44.9%, by placing 17.25 million shares at a price of €62.25 per share. Bayer AG's
interest in Covestro was reduced by a further 4 percentage points through the contribution
of Covestro shares to the Bayer Pension Trust e. V. In addition, Bayer has issued
€1 billion in bonds maturing in 2020 that can be redeemed in cash, Covestro shares
or a combination of the two. Covestro continues to be fully consolidated in Bayer's
financial statements, as, even with these transactions having been completed, Bayer
will still hold the de facto majority at a Covestro stockholders' meeting. On June 30, 2017, Bayer filed an application with the European Commission seeking
approval for the planned acquisition of Monsanto, representing a further significant
milestone in the transaction. Bayer also announced on June 30, 2017, that it was revising its annual guidance. 1. Overview of Sales, Earnings and Financial Position1.1 Earnings Performance of the Bayer Group1Second quarter of 2017Group salesSales of the Bayer Group increased by 1.9% (Fx & portfolio adj.) to €12,193 million
in the second quarter of 2017 (reported: + 3.0%). Germany accounted for €1,216 million
of this figure. Sales of the Life Science businesses declined by 2.8% (Fx & portfolio
adj.) to €8,714 million. Pharmaceuticals posted sales growth of 4.4% (Fx & portfolio adj.) to €4,304 million,
mainly due to our key growth products continuing to deliver strong performance. Sales
at Consumer Health declined year on year, falling by 2.2% (Fx. & portfolio adj.) to
€1,542 million. Sales at Crop Science fell by a significant 15.8% (Fx & portfolio
adj.) to €2,163 million, primarily due to its Brazil business. Excluding Brazil, sales
matched the prior-year level. Animal Health achieved growth of 2.1% (Fx & portfolio
adj.), with sales rising to €450 million. Sales at Covestro improved considerably,
increasing by 15.8% (Fx & portfolio adj.) to €3,479 million. EBITDA before special itemsAt €3,056 million, EBITDA before special items of the Bayer Group matched the prior-year
level (+ 0.1%). EBITDA before special items at Pharmaceuticals improved by a very
encouraging 9.5% to €1,481 million. At Consumer Health, EBITDA before special items
declined by 4.3% to €314 million. EBITDA before special items at Crop Science decreased
by a significant 52.2% to €317 million, mainly due to provisions for product returns
in Brazil. EBITDA before special items of Animal Health climbed by 16.0% to €116 million.
Overall, EBITDA before special items of our Life Science businesses declined by 10.5%
to €2,247 million. Covestro raised EBITDA before special items by a considerable 49.0%
to €809 million. Depreciation, amortization and special itemsDepreciation, amortization and impairment losses were 2.2% higher in the second quarter
of 2017, at €832 million (Q2 2016: €814 million), comprising €422 million (Q2 2016:
€447 million) in amortization and impairments on intangible assets and €410 million
(Q2 2016: €367 million) in depreciation and impairments on property, plant and equipment.
Impairment losses and impairment loss reversals amounted to €126 million, of which
€122 million (Q2 2016: €0 million) constituted special items. In addition, an amount
of €10 million was included in special items as accelerated depreciation. EBITEBIT of the Bayer Group came to €2,151 million, matching the prior-year period (Q2
2016: €2,138 million; + 0.6%). This figure reflected net special charges of €205 million
(Q2 2016: €104 million). These mainly comprised €118 million in value adjustments
in the Pharmaceuticals segment, €47 million in charges in conjunction with the agreed
acquisition of Monsanto, and €37 million in charges related to efficiency improvement
programs. EBIT before special items moved forward by 5.1% to €2,356 million (Q2 2016:
€2,242 million). In the second quarter of 2017, the following special effects were taken into account
in calculating EBIT and EBITDA: A 1Special Items Reconciliation1
Net incomeIncluding a financial result of minus €405 million (Q2 2016: minus €314 million),
income before income taxes was €1,746 million (Q2 2016: €1,824 million). After income
tax expense of €417 million (Q2 2016: €431 million) and adjusting for income from
discontinued operations after income taxes and noncontrolling interest, net income
for the second quarter of 2017 amounted to €1,224 million (Q2 2016: €1,380 million). Core earnings per shareEarnings per share (total) declined by 16.2% in the second quarter of 2017, to €1.40
(Q2 2016: €1.67), while core earnings per share from continuing operations fell by
12.6% to €1.81 (Q2 2016: €2.07). Material effects included the reduction of our interest
in Covestro and the increased number of shares following the issuance of the mandatory
convertible notes. A 2Core Earnings per Share1
In calculating net income and core earnings per share, the sale of a further 17.25
million shares in Covestro AG to institutional investors in the second quarter, at
a price of €62.25 per share, was taken into consideration. In addition, 8 million
shares of Covestro AG were deposited in Bayer Pension Trust e.V. at a price of €63.04
per share. Bayer thus reduced its interest from 53.3% to 40.9% of the issued stock. As of June 30, 2017, personnel expenses rose by 1.3% compared with June 30, 2016,
to €2,826 million (Q2 2016: €2,789 million). As of the closing date, the number of
employees in the Bayer Group was largely unchanged year on year, at 115,680 (June
30, 2016: 115,576; + 0.1%). First half of 2017Group salesSales of the Bayer Group in the first half of 2017 increased by 5.7% (Fx & portfolio
adj.) to €25,437 million (reported: + 7.4%), with Germany accounting for €2,610 million
of this figure. Our Life Science businesses grew sales by 1.1% (Fx & portfolio adj.)
to €18,394 million. Sales of Pharmaceuticals advanced by 5.8% (Fx & portfolio adj.) to €8,567 million.
At Consumer Health, sales were flat year on year at €3,143 million (Fx & portfolio
adj.: + 0.2%). Crop Science sales declined by 5.4% (Fx & portfolio adj.) to €5,283
million. Animal Health posted a 2.5% increase (Fx & portfolio adj.) in sales to €890
million. At Covestro, sales improved by a substantial 19.6% (Fx & portfolio adj.)
to €7,043 million. EBITDA before special itemsEBITDA before special items of the Bayer Group advanced by 7.9% to €6,949 million
(H1 2016: €6,441 million). Pharmaceuticals increased EBITDA before special items by
a substantial 14.2% to €2,983 million. EBITDA before special items of Consumer Health
came to €706 million, matching the prior-year period (- 0.7%). EBITDA before special
items at Crop Science declined by a substantial 18.3% to €1,432 million, while Animal
Health registered a significant earnings increase of 13.1% to €251 million. Overall,
EBITDA before special items of the Life Science businesses declined slightly by 1.7%
compared with the prior-year period, to €5,301 million. Covestro raised EBITDA before
special items by a considerable 57.4% to €1,648 million. Depreciation, amortization and special itemsIn the first half of 2017, depreciation, amortization and impairments amounted to
€1,562 million (H1 2016: €1,853 million), comprising €771 million (H1 2016: €1,114
million) in amortization and impairments on intangible assets and €791 million (H1
2016: €739 million) in depreciation and impairments on property, plant and equipment.
Impairment losses and impairment loss reversals amounted to €166 million (H1 2016:
€298 million). Impairment losses and impairment loss reversals in the amount of €160
million (H1 2016: €244 million) as well as accelerated depreciation in the amount
of €10 million constituted special items. EBITEBIT of the Bayer Group rose by a substantial 18.1% to €5,267 million (H1 2016: €4,458
million), after net special charges of €290 million (H1 2016: €376 million). These
mainly comprised €151 million in value adjustments, €68 million in charges in conjunction
with the agreed acquisition of Monsanto, and €63 million in charges related to efficiency
improvement programs. EBIT before special items moved forward by a significant 15.0%
to €5,557 million (H1 2016: €4,834 million). Net incomeIncluding a financial result of minus €754 million (H1 2016: minus €629 million),
income before income taxes amounted to €4,513 million (H1 2016: €3,829 million). The
financial result comprised in particular a net interest expense of €268 million (H1
2016: €260 million), currency hedging costs in the amount of €233 million (H1 2016:
€177 million), and interest cost of €115 million (H1 2016: €143 million) for pension
and other provisions. After tax expense of €1,012 million (H1 2016: €905 million),
income after income taxes was €3,501 million (H1 2016: €2,924 million). Adjusted for
income from discontinued operations after income taxes and noncontrolling interest,
net income came to €3,307 million (H1 2016: €2,891 million). Core earnings per shareEarnings per share (total) increased to €3.79 (H1 2016: €3.50), while core earnings
per share from continuing operations amounted to €4.44, in line with the prior-year
period (H1 2016: €4.42). 1.2 Business Development by SegmentPharmaceuticalsA 3Key Data - Pharmaceuticals
2016 figures restated; Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted Second quarter of 2017SalesSales of Pharmaceuticals increased by 4.4% (Fx & portfolio adj.) to €4,304 million
in the second quarter of 2017. Our key growth products Xarelto™, Eylea™, Xofigo™,
Stivarga™ and Adempas™ once again delivered strong performance, with their combined
sales rising by 16.6% (Fx adj.) to €1,555 million (Q2 2016: €1,332 million). Combined
sales of the 15 best-selling Pharmaceuticals products advanced by 7.7% (Fx adj.).
Our Pharmaceuticals business expanded in all regions. A 4Best-Selling Pharmaceuticals Products
1
Fx adj. = currency-adjusted; for definition see Annual Report 2016, A 2.4 "Alternative
Performance Measures Used by the Bayer Group." Sales by product
EarningsEBITDA before special items of Pharmaceuticals improved by a very encouraging 9.5% to €1,481 million in the second quarter of 2017 (Q2 2016: €1,352 million). Positive earnings effects resulted primarily from higher volumes, while the cost of goods sold and expenses for research and development were lower. EBIT increased by a substantial 11.5% to €1,102 million, and included special charges of €120 million (Q2 2016: €11 million). These largely comprised €69 million in impairments on intangible assets in the area of oncology (OncoMed), and €49 million in value adjustments in the area of women's health. A 5Special Items1 Pharmaceuticals
First half of 2017SalesSales of Pharmaceuticals rose by 5.8% (Fx & portfolio adj.) to €8,567 million in the
first half of 2017. Our key growth products Xarelto™, Eylea™, Stivarga™, Xofigo™ and
Adempas™ delivered strong performance, with their combined sales rising by 18.2% (Fx
adj.) to €3,000 million (H1 2016: €2,519 million). Pharmaceuticals sales developed
positively in all regions. EarningsEBITDA before special items improved by a substantial 14.2% in the first half of 2017, to €2,983 million. This positive earnings performance was the result of the good development of business, while the cost of goods sold and expenses for research and development were lower. In addition, selling expenses increased at a slower rate than sales. EBIT increased substantially, rising by 37.7% to €2,321 million. Special charges amounted to €156 million (H1 2016: €242 million) and were primarily the result of value adjustments. Consumer HealthA 6Key Data - Consumer Health
2016 figures restated; Fx & p adj. = currency- and portfolio-adjusted; Fx adi. = currency-adjusted Second quarter of 2017SalesSales of Consumer Health in the second quarter of 2017 fell by 2.2% (Fx & portfolio
adj.) to €1,542 million. We recorded substantial declines in sales in North America,
particularly in the United States, due to the difficult market environment. In contrast,
we expanded our business in Latin America and Europe / Middle East / Africa. A 7Best-Selling Consumer Health Products
1
Fx adj. = currency-adjusted; for definition see Annual Report 2016, A 2.4 "Alternative
Performance Measures Used by the Bayer Group." Sales by product
EarningsEBITDA before special items of Consumer Health declined by 4.3% to €314 million in the second quarter of 2017 (Q2 2016: €328 million). The fall in earnings is mainly attributable to lower volumes and the higher cost of goods sold, which resulted in part from inventory write-offs. EBIT increased by 2.6% to €195 million, and included special charges of €15 million (Q2 2016: €32 million). A 8Special Items1 Consumer Health
First half of 2017SalesIn the first half of 2017, Consumer Health posted sales of €3,143 million (Fx & portfolio
adj. + 0.2%). Business developed positively in Europe in particular, while sales fell
in North America due to a difficult market environment in the United States. EarningsEBITDA before special items decreased by 0.7% in the first half of 2017, to €706 million (H1 2016: €711 million). Earnings contributions from the development of business stood against the higher cost of goods sold, which was due in part to inventory write-offs. EBIT moved ahead by a clear 9.2% to €473 million (H1 2016: €433 million). Special charges amounted to €24 million (H1 2016: €64 million). Crop ScienceA 9Key Data - Crop Science
2016 figures restated; Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted Second quarter of 2017SalesSales of Crop Science in the second quarter of 2017 fell by 15.8% (Fx & portfolio
adj.) to €2,163 million. This decline is mainly due to significantly higher provisions
for product returns - specifically crop-protection products - in Brazil. At the end
of the harvest season, regular stocktaking revealed high channel inventories in the
Brazilian market, requiring measures to be taken to normalize the situation. Excluding
the €428 million decline in sales in Brazil, business at Crop Science was up slightly
year on year on a currency-adjusted basis. Environmental Science delivered positive
performance, in part due to the delivery of products to the company that acquired
our consumer business. A 10Sales by Business Unit
Fx & p adj. = currency- and portfolio-adjusted; Sales by region
EarningsEBITDA before special items of Crop Science declined by 52.2% to €317 million in the second quarter of 2017 (Q2 2016: €663 million), in particular due to the situation in Brazil, where we recorded a substantial negative impact on earnings in the amount of €355 million in total. This included provisions for product returns in the amount of €173 million, impairment losses recognized on receivables in the amount of €53 million, inventory write-offs in the amount of €56 million, and other effects totaling €73 million. Excluding our business in Brazil, earnings were up slightly year on year. EBIT decreased by 77.1% to €117 million, and included special charges in the amount of €95 million (Q2 2016: €30 million) related mainly to the agreed acquisition of Monsanto and the completion of a divestiture project. A 11Special Items1 Crop Science
First half of 2017SalesSales of Crop Science in the first half of 2017 declined by 5.4% (Fx & portfolio adj.) to €5,283 million. Sales fell at Fungicides and Insecticides in particular due to the aforementioned adjustments made to provisions for product returns and weak business in Brazil. In contrast, we achieved gains at Seeds and Environmental Science. Higher sales in North America and Europe / Middle East / Africa were insufficient to offset the substantial decline in business in Latin America. Sales in Asia / Pacific came in at the prior-year level. Excluding Brazil, sales increased slightly overall. EarningsEBITDA before special items of Crop Science declined by 18.3% to €1,432 million (H1 2016: €1,752 million) in the first half of 2017, significantly weighed down by the aforementioned effects in Brazil. Excluding Brazil, earnings were higher than in the prior-year period. EBIT declined by 25.9% to €1,087 million. Earnings were held back by special charges of €132 million (H1 2016: €33 million) largely related to the agreed acquisition of Monsanto, the completion of a divestiture project and efficiency improvement programs. Animal HealthA 12Key Data - Animal Health
201 6 figures restated; Fx & p adj. = currency- and portfolio-adjusted; Fx adj. =
currency-adjusted Second quarter of 2017SalesSales of Animal Health in the second quarter of 2017 moved ahead by 2.1% (Fx & portfolio
adj.) to €450 million. The development of business in the Asia / Pacific region was
encouraging. In North America, the Cydectin™ product portfolio that was acquired in
January 2017 contributed to sales growth on a currency-adjusted basis. We recorded
a slight increase in sales in Europe / Middle East / Africa on a currency-adjusted
basis, while the performance of our Latin America business matched the prior-year
period. A 13Best-Selling Animal Health Products
Sales by product
EarningsEBITDA before special items of Animal Health increased by 16.0% to €116 million in the second quarter of 2017 (Q2 2016: €100 million). Positive earnings contributions resulted from price increases, the lower cost of goods sold as well as the Cydectin™ business that Bayer acquired. These more than offset a decline in volumes and slightly higher expenses for research and development. EBIT climbed by 15.1% to €107 million, with no special items (Q2 2016: €0 million) recorded. A 14Special Items1 Animal Health
First half of 2017SalesSales of Animal Health rose by 2.5% (Fx & portfolio adj.) to €890 million in the first
half of 2017. Development in the Asia / Pacific region was especially positive. We
also recorded sales gains in North America and Europe / Middle East / Africa, while
business in Latin America declined slightly on a currency-adjusted basis. EarningsEBITDA before special items increased by 13.1% to €251 million in the first half of 2017. Performance was driven by positive price effects and the newly acquired Cydectin™ business. This development stood against higher expenses for research and development. EBIT improved by 12.6% to €233 million, with no special items (Q2 2016: special charges of €1 million) recorded. CovestroA 15Key Data - Covestro
2016 figures restated; Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted Second quarter of 2017SalesSales of Covestro in the second quarter of 2017 increased by 15.8% (Fx & portfolio
adj.) to €3,479 million. Selling prices were much higher overall, especially at Polyurethanes,
while volumes matched the prior-year period overall. A 16Sales by Business Unit
Fx & p adj. = currency- and portfolio-adjusted; for definition see Annual Report 2016,
A 2.4 "Alternative Performance Measures Used by the Bayer Group." Sales by business unit
EarningsEBITDA before special items of Covestro improved by 49.0% to €809 million in the second quarter of 2017 (Q2 2016: €543 million). Substantially higher selling prices more than offset the effect of increased raw material prices. EBIT increased by 87.5% to €688 million, and included a special gain in the amount of €39 million (Q2 2016: €0 million) resulting from the sale of the segment's North American spray polyurethane foam system house. A 17Special Items1 Covestro
First half of 2017SalesSales of Covestro increased by 19.6% (Fx & portfolio adj.) in the first half of 2017
compared with the prior-year period, to €7,043 million, due to significantly higher
selling prices, especially at Polyurethanes. All business units reported higher volumes. EarningsEBITDA before special items of Covestro improved by 57.4% to €1,648 million in the first half of 2017 (H1 2016:
€1,047 million). A significant increase in selling prices and higher volumes more
than offset higher raw material costs. EBIT climbed by 95.9% to €1,377 million, and included special gains of €56 million (H1
2016: €0 million) related to the aforementioned sale and the decision made in the
first quarter of 2017 to postpone the closure of a production facility until further
notice. 1.3 Asset and Financial Position of the Bayer Group Statement of Cash FlowsA 18Bayer Group Summary Statements of Cash Flows
2016 figures restated Net cash provided by operating activities
Net cash used in investing activities
Net cash provided by (used in) financing activities
Liquid assets and net financial debtA 19Net Financial Debt1
1
For definition see Annual Report 2016, A 2.4 "Alternative Performance Measures Used
by the Bayer Group."
Asset and capital structureA 20Bayer Group Summary Statements of Financial Position
2. Research, Development, InnovationBayer Group expenses for research and development rose by 3.0% (Fx adj.) to €1,165
million in the second quarter of 2017, with the Life Science businesses accounting
for €1,097 million (Fx adj. +2,6%) of this figure. A 21Research and Development Expenses
2016 figures restated PharmaceuticalsWe are conducting clinical trials with a number of drug candidates from our research
and development pipeline. The following table shows our most important drug candidates currently in Phase II
of clinical testing: A 22Research and Development Projects (Phase II)1
1
As of July 3, 2017 The nature of drug discovery and development is such that not all compounds can be
expected to meet the predefined project goals. It is possible that any or all of the
projects listed above may have to be discontinued due to scientific and / or commercial
reasons and will not result in commercialized products. It is also possible that the
requisite U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA)
or other regulatory approvals will not be granted for these compounds. Moreover, we
regularly review our research and development pipeline so that we can give priority
to advancing the most promising pharmaceuticals projects. Based on the results of the GEMINI trial conducted by Janssen Research & Development,
LLC, which had investigated rivaroxaban (tradename: Xarelto™) used in connection with
a single antiplatelet therapy (SAPT) for the secondary prophylaxis of acute coronary
syndrome (ACS), the decision was made to no longer pursue the development of rivaroxaban
in this indication. The following table shows our most important drug candidates currently in Phase III
of clinical testing: A 23Research and Development Projects (Phase III)1
1
As of July 03, 2017 The nature of drug discovery and development is such that not all compounds can be
expected to meet the predefined project goals. It is possible that any or all of the
projects listed above may have to be discontinued due to scientific and / or commercial
reasons and will not result in commercialized products. It is also possible that the
requisite U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA)
or other regulatory approvals will not be granted for these compounds. Moreover, we
regularly review our research and development pipeline so that we can give priority
to advancing the most promising pharmaceuticals projects. In July 2017, Bayer initiated the Phase III clinical trial program ASTEROID, which
is investigating the development candidate vilaprisan in women with symptomatic uterine
fibroids. The product of Bayer's research efforts, vilaprisan is a novel oral and
selective progesterone receptor modulator that is aimed at treating uterine fibroids
long term. The most important drug candidates in the approval process are: A 24Main Products Submitted for Approval1
1
As of July 3, 2017 In April 2017, Bayer and its development partner Janssen Research & Development submitted
an additional dose option for the oral Factor Xa inhibitor rivaroxaban (tradename:
Xarelto™) to the U.S. Food and Drug Administration (FDA), seeking an expansion of
indications. The application is supported by data from the EINSTEIN CHOICE trial.
The new dose of 10mg of rivaroxaban once a day is to supplement the current therapy
of 20mg once a day and is intended for use as an anticoagulation therapy to reduce
the risk of recurrent venous thromboembolism after at least six months of standard
therapy with anticoagulants. In May 2017, the FDA granted priority review status to the development candidate copanlisib
in the registration process, based on the Phase II data presented in the first quarter
of 2017. The substance is being reviewed for the treatment of relapsed or refractory
follicular lymphoma. In April and June 2017, Bayer received approvals from the FDA and Japanese Ministry
of Health, Labour and Welfare (MHLW) for the use of its oral multikinase inhibitor
Stivagra™ (active ingredient: regorafenib) for the second-line treatment of patients
with hepatocellular carcinoma who previously had been treated with Nexavar™ (active
ingredient: sorafenib). Stivarga™ is the first drug product to show a significant
improvement in overall survival in the second-line treatment of patients with hepatocellular
carcinoma. In June 2017, the European Committee for Medicinal Products for Human Use recommended
the approval of Bayer's cancer drug Stivarga™ (active ingredient: regorafenib) for
the treatment of adult patients with hepatocellular carcinoma in the European Union
who had previously been treated with Nexavar™ (active ingredient: sorafenib). The
European Commission is expected to make a decision in the third quarter of 2017. CollaborationsOn April 6, 2017, Bayer decided to not exercise its option to further develop and
market Wnt signaling pathway inhibitors, a class of biologics, as part of its collaboration
with OncoMed Pharmaceuticals Inc., United States. Crop ScienceIn April 2017, we received regulatory approval for the biological nematicide BioAct™
Prime DC in Greece. The new substance is intended for use in a variety of fruit and
vegetables and directly targets eggs and larvae from nematode pests. The product is
scheduled to be launched in Greece in 2017 and there are plans to gain approvals in
other European countries, too. In June 2017, Bayer and KWS SAAT SE, Germany - in line with their research cooperation
which began in 2012 - granted a long-term license to the Belgian company SESVanderHave
for their new CONVISO™SMART sugar beet cultivation system. The technology, which is
based on conventionally cultivated sugar beet varieties that are tolerant to certain
herbicides, makes weed management easier. It will initially be made available to farmers
in 2018, mainly in Eastern and Northern Europe, and is to be introduced in the following
years in Germany, France and Poland, among other countries. We also signed a two-year research agreement with the Shanghai Institutes for Biological
Sciences (SIBS) of the Chinese Academy of Sciences in June 2017. The purpose of the
agreement is to increase wheat yields using new mathematical models and computer simulations
for more efficient photosynthesis. The improvement in photosynthesis is considered
to be a promising approach to considerably increasing plant productivity. In June 2017, Bayer also signed an agreement with the Sumitomo Chemical Company, which
is headquartered in Tokyo, Japan, for fungicide mixes used to control soybean diseases
in Brazil. The companies plan to develop an effective substance to control widespread
plant diseases such as soybean rust by combining a new fungicide produced by Sumitomo
Chemical with established Bayer fungicides. Both companies expect to file a product
registration application at the end of 2017. CovestroCovestro and its partners have developed a new procedure for producing the basic chemical
aniline using industrial sugar. The chemical is used in the production of plastics.
This means that benzene, a raw material derived from crude oil, can be replaced by
biomass. The laboratory-tested procedure is now to be transferred to a larger pilot
facility with the goal of manufacturing aniline on an industrial scale using renewable
raw materials. 3. Report on Future Perspectives and on Opportunities and Risks3.1 Future Perspectives3.1.1 Economic OutlookA 25Economic Outlook1
2016 figures restated 1
Real growth of gross domestic product, source: IHS Global Insight As of June 2017 The economic prospects further improved in the first half of 2017, and the global
economy is likely to expand at a faster pace than in the previous year. In the United
States, particularly, we expect more favorable economic development. We now expect
a slightly faster pace of growth in the European Union despite uncertainty surrounding
future political development there. Economic output in the Emerging Markets will probably
pick up considerably overall compared with the previous year. We continue to expect
strong growth in China but at a slightly slower pace. A 26Economic Outlook for the Segments1
2016 figures restated As of June 2017 In 2017, Covestro expects a continuation of the growth trend in its main customer
industries - construction, electrical engineering and electronics, and furniture.
Growth in the automotive industry is still expected to be weaker than in the previous
year. 3.1.2 Corporate OutlookDue to the current business and currency development, we are adjusting our forecast
for the fiscal year 2017. The forecast for the second half is based on the exchange rates as of June 30, 2017,
including a rate of US$1.14 (previously: US$1.07) to the euro. A 1% appreciation (depreciation)
of the euro against all other currencies would decrease (increase) sales on an annual
basis by €300 million and EBITDA before special items by €80 million. This results in the following changes overall for the Bayer Group: Sales are now expected
to increase to more than €49 billion (previously: around €51 billion). This now corresponds
to a mid-single-digit (previously: mid- to high-single-digit) percentage increase
on a currency- and portfolio-adjusted basis. EBITDA before special items is now targeted
to increase by a high-single-digit percentage (previously: low-teens percentage).
We now aim to grow core earnings per share from continuing operations by a low- to
mid-single-digit percentage (previously: mid- to high-single-digit percentage). Here
it must be noted that Bayer's interest in Covestro amounts to only 41 % as of June
2017 (previously: 53%). Excluding capital and portfolio measures, net financial debt
is targeted to be around €7 billion at the end of 2017 (previously: around €8 billion). We are now budgeting for sales of between €35 billion and €36 billion (previously:
approximately €37 billion) for our Life Science businesses. This corresponds to a
low-single-digit percentage (previously: midsingle-digit percentage) increase on a
currency- and portfolio-adjusted basis. We expect EBITDA before special items to come
in slightly above the level of the previous year (previously: rise by a mid- to highsingle-digit
percentage). Despite negative currency development, we confirm the forecast we published in February
for Pharmaceuticals and continue to expect sales of more than €17 billion. This corresponds
to a mid-single-digit percentage increase on a currency- and portfolio-adjusted basis.
As before, we plan to raise sales of our key growth products to more than €6 billion.
We continue to expect a high-single-digit percentage increase in EBITDA before special
items. There is no change in our expectation of further improving the EBITDA margin
before special items. For Consumer Health, we forecast a weak second half of the year and now expect to
generate full-year sales of about €6 billion (previously: more than €6 billion). This
would be in line with the prior-year level on both a reported and a currency- and
portfolio-adjusted basis (previously: low- to mid-single-digit percentage increase
on a currency- and portfolio-adjusted basis). We now expect EBITDA before special
items to decline by a high-single-digit percentage (previously: increase by a low-
to mid-single-digit percentage). We are now budgeting for sales of below €10 billion (previously: more than €10 billion)
for Crop Science. This corresponds to low-single-digit-percentage decline on a currency-
and portfolio-adjusted basis (previously: low-single-digit percentage increase). We
now expect EBITDA before special items to decline by a mid-teens percentage (previously:
at the prior-year level). We confirm the forecasts published in February and April 2017 for Animal Health, the
Reconciliation and Covestro. This also applies to the forecasts for the other key
data. 3.2 Opportunities and risksAs a global enterprise with a diversified portfolio, the Bayer Group is exposed to
a wide range of internal or external developments and events that could significantly
impact the achievement of our financial and nonfinancial objectives. Bayer regards opportunity and risk management as an integral part of corporate governance.
Our risk management process and the opportunities / risks are outlined in detail in
the Annual Report 2016 (Combined Management Report, A 3.2 "Opportunity and Risk Report").
For risks related to the acquisition of Monsanto Company, United States, we refer
specifically to A 3.2.3 "Planned Acquisition of Monsanto." There have been no material
changes to Bayer's overall risk situation. From the current perspective, no risks have been identified that could endanger the
Bayer Group's continued existence. There are also no risks with mutually reinforcing
dependencies that could combine to endanger the Group's continued existence. Significant developments that have occurred in respect of the legal risks since publication
of the Bayer Annual Report 2016 (Note [32] to the Consolidated Financial Statements)
are described in the Notes to the Condensed Consolidated Interim Financial Statements
under "Legal Risks." Condensed Consolidated Interim Financial Statements as of June 30, 2017Bayer Group Consolidated Income StatementsB 1
Bayer Group Consolidated Statements of Comprehensive IncomeB 2
1
Total changes recognized outside profit or loss Bayer Group Consolidated Statements of Financial PositionB 3
Bayer Group Consolidated Statements of Cash FlowsB 4
2016 figures restated Bayer Group Consolidated Statements of Changes in EquityB 5
Notes to the Condensed Consolidated Interim Financial Statements of the Bayer Group as of June 30, 2017Key Data by Segment and RegionB 6Key Data by Segment
B 7Key Data by Segment
1
For definition see Annual Report 2016, A 2.4 "Alternative Performance Measures Used
by the Bayer Group." B 8Key Data by Region
2016 figures restated B 9Key Data by Region
2016 figures restated 1
For definition see Annual Report 2016, A 2.4 "Alternative Performance Measures Used
by the Bayer Group." Explanatory NotesAccounting policiesThe consolidated interim financial statements as of June 30, 2017, were prepared in
condensed form in compliance with IAS 34 according to the International Financial
Reporting Standards (IFRS) of the International Accounting Standards Board (IASB),
London, which are endorsed by the European Union, and the Interpretations of the IFRS
Interpretations Committee in effect at the closing date. Reference should be made as appropriate to the Notes to the Consolidated Financial
Statements for the 2016 fiscal year, particularly with regard to the main recognition
and valuation principles. Published financial reporting standards that have not yet been appliedIFRS 15 (Revenue from Contracts with Customers) is the new standard for revenue recognition
that is to be applied for annual reporting periods beginning on or after January 1,
2018. Bayer will implement IFRS 15 on the basis of the modified retrospective method, accounting
for the aggregate amount of any transition effects by way of an adjustment to retained
earnings as of January 1, 2018, and presenting the comparative period in line with
previous rules. All of the established business models for the Bayer Group's Life
Science divisions were examined in the course of the implementation project. The previous
assessment that the new standard is not expected to materially affect the timing of
revenue recognition for the transactions concerned or their components has been confirmed
for companies examined since then. The analysis has not yet been completed in a number
of material consolidated companies. Possible but currently not quantifiable effects
in the Covestro segment can result with regard to the timing of revenue recognition
for certain storage agreements, a number of customer-specific products and the provision
of services such as transport or freight services. Furthermore, the evaluation of
certain individual licensing agreements has not yet been completed for Bayer. With
regard to total Group sales, there are indications of immaterial transition effects
due to the different accounting of milestone payments in connection with right-to-access
licenses that would result in an increase in retained earnings on the transition date.
IFRS 15 clarifies the allocation of individual topics to (new) line items in the statement
of financial position and to functional cost items in the income statement, and whether
gross or net amounts are to be presented. Determination of the effects on the level
of sales or selling expenses has not yet been completed. Based on current knowledge,
however, we do not anticipate any material effects on these items. Overall, based
on current knowledge, we do not anticipate any material effects on the presentation
of the Life Science businesses' financial position or results of operations, or on
earnings per share. A similar statement concerning the Covestro segment cannot yet
be made at the present point in time. Changes in underlying parametersChanges in the underlying parameters relate primarily to currency exchange rates and
the interest rates used to calculate pension obligations. The exchange rates for major currencies against the euro varied as follows: B 10Exchange Rates for Major Currencies
The most important interest rates used to calculate the present value of pension obligations
are given below: B 11Discount Rate for Pension Obligations
Segment reportingSince January 1, 2016, the Bayer Group has comprised the five reportable segments
Pharmaceuticals, Consumer Health, Crop Science, Animal Health and Covestro. The following table shows the reconciliation of EBITDA before special items of the
above-mentioned segments and the reconciliation to income before income taxes of the
Group: B 12Reconciliation of Segments' EBITDA Before Special Items to Group Income Before Income Taxes
Scope of consolidationChanges in the scope of consolidationThe consolidated financial statements as of June 30, 2017, included 293 companies
(December 31, 2016: 301 companies). As in the statements as of December 31, 2016,
one of these companies was accounted for as a joint operation in line with Bayer's
interest in its assets, liabilities, revenues and expenses in accordance with IFRS
11 (Joint Arrangements). Six (December 31, 2016: six) joint ventures and five (December
31, 2016: five) associates were accounted for in the consolidated financial statements
using the equity method according to IAS 28 (Investments in Associates and Joint Ventures). Acquisitions, divestitures and discontinued operationsAcquisitionsOn January 3, 2017, Bayer acquired the Cydectin™ portfolio in the United States from
Boehringer Ingelheim Vetmedica Inc., St. Joseph, United States. The acquisition comprises
the CYDECTIN Pour-On, CYDECTIN Injectable and CYDECTIN Oral Drench endectocides for
cattle and sheep. The acquisition is intended to strengthen the antiparasitics portfolio
in the United States, and will see endectocides added to the portfolio. A purchase
price of €158 million was agreed, which is subject to the usual price adjustment mechanisms.
The purchase price was provisionally allocated mainly to trademarks and goodwill.
The purchase price allocation currently remains incomplete pending compilation and
review of the relevant financial information. It is therefore possible that changes
will be made in the allocation of the purchase prices to the individual assets. The effects of this transaction - as of the acquisition date - on the Group's assets
and liabilities in the first half of 2017 are shown in the following table. The transaction
resulted in the following cash outflow: B 13Acquired Assets, Assumed Liabilities and Adjustments (Fair Values at the Respective Acquisition Dates)
Planned acquisitionsDetails of the planned acquisition of Monsanto are given in our Annual Report 2016. DivestmentsOn April 3, 2017, Covestro completed the sale of a North American spray polyurethane
foam system house to Accella Polyurethane Systems LLC, Maryland Heights, United States.
A purchase price of €47 million was agreed. Income of €39 million was reported in
special items. On April 1, 2017, Consumer Health completed the sale of a production facility in Pointe-Claire,
Canada, to Famar Montréal Inc., Montréal, Canada. The base sale price was CAD1 million. The effects of these divestments made in the first half of 2017 were as follows: B 14Divested Assets and Liabilities
The divested assets were reported in previous quarters as assets held for sale. Discontinued operationsThe sale of the Diabetes Care business to Panasonic Healthcare Holdings Co., Ltd.,
Tokyo, Japan, for around €1 billion was completed on January 4, 2016. The sale includes
the leading Contour™ portfolio of blood glucose monitoring meters and strips, as well
as other products such as Breeze™2, Elite™ and Microlet™ lancing devices. The sale of the Diabetes Care business also comprises further significant obligations
by Bayer that will be fulfilled over a period of up to two years subsequent to the
date of divestment. The sale proceeds will be recognized accordingly over this period
and reported as income from discontinued operations. Deferred income has been recognized
in the statement of financial position and will be dissolved as the obligations are
fulfilled. An amount of €287 million was recognized in sales in the first half of
2017. The obligations to be fulfilled over a period of up to two years after the divestment
of the Diabetes Care business are also reported as discontinued operations in the
income statement and the statement of cash flows. They resulted in sales of €25 million
in the first half of 2017. The items in the statement of financial position pertaining to the Diabetes Care business
are shown in the segment reporting under "All Other Segments." In addition to the
aforementioned deferred income (€177 million), the statement of financial position
includes other receivables (net: €60 million), deferred tax assets (net: €29 million),
income tax liabilities (€56 million) and other provisions (€4 million). The sale of the Consumer business (CS Consumer) of Bayer's Environmental Science unit
to SBM Développement SAS, Lyon, France, was completed on October 4, 2016. These activities
have been reported as discontinued operations since the second quarter of 2016. The income statements of the discontinued operations for the second quarter of 2017
are given below: B 15Income Statements for Discontinued Operations
1
EBIT = income after income taxes, plus income taxes, plus financial result The income statements of the discontinued operations for the first half of 2017 are
given below: B 16Income Statements for Discontinued Operations
1
EBIT = income after income taxes, plus income taxes, plus financial result In the second quarter of 2017, the discontinued operations affected the Bayer Group
statement of cash flows as follows: B 17Statements of Cash Flows for Discontinued Operations
In the first half of 2017, the discontinued operations affected the Bayer Group statement
of cash flows as follows: B 18Statements of Cash Flows for Discontinued Operations
As no cash is assigned to discontinued operations, the balance of the cash provided
is deducted again in financing activities. Financial instrumentsB 19Carrying Amounts and Fair Values of Financial Instruments
B 20Carrying Amounts and Fair Values of Financial Instruments
The preceding two tables show the carrying amounts and fair values of financial assets
and liabilities for each financial instrument category and a reconciliation to the
corresponding line items in the statements of financial position. Since the line items
"Other receivables," "Trade accounts payable" and "Other liabilities" contain both
financial instruments and nonfinancial assets or liabilities (such as other tax receivables
or advance payments for services to be received in the future), the reconciliation
is shown in the column headed "Nonfinancial assets / liabilities." The loans and receivables reflected in other financial assets and the liabilities
measured at amortized cost also include receivables and liabilities under finance
leases in which Bayer is the lessor or lessee and which are therefore measured in
accordance with IAS 17. Because of the short maturities of most trade accounts receivable and payable, other
receivables and liabilities and cash and cash equivalents, their carrying amounts
at the closing date do not significantly differ from the fair values. The fair values of loans and receivables, held-to-maturity financial investments and
of financial liabilities carried at amortized cost that are given for information
are the present values of the respective future cash flows. The present values are
determined by discounting the cash flows at a closing-date interest rate, taking into
account the term of the assets or liabilities and the creditworthiness of the counterparty.
Where a market price is available, however, this is deemed to be the fair value. The fair values of available-for-sale financial assets correspond to quoted prices
in active markets (Level 1), are determined using valuation techniques based on observable
market data as of the end of the reporting period (Level 2) or are the present values
of the respective future cash flows, determined on the basis of unobservable inputs
(Level 3). The fair values of derivatives for which no publicly quoted prices exist in active
markets (Level 1) are determined using valuation techniques based on observable market
data as of the end of the reporting period (Level 2). In applying valuation techniques,
credit value adjustments are determined to allow for the contracting party's credit
risk. Currency and commodity forward contracts are measured individually at their forward
rates or forward prices on the closing date. These depend on spot rates or prices,
including time spreads. The fair values of interest-rate hedging instruments and cross-currency
interest-rate swaps were determined by discounting future cash flows over the remaining
terms of the instruments at market rates of interest, taking into account any foreign
currency translation as of the closing date. Fair values measured using unobservable inputs are categorized within Level 3 of the
fair value hierarchy. This applies to certain available-for-sale debt or equity instruments,
in some cases to the fair values of embedded derivatives, and to obligations for contingent
consideration in business combinations. Credit risk is frequently the principal unobservable
input used to determine the fair values of debt instruments classified as available-for-sale
financial assets by the discounted cash flow method. Here the credit spreads of comparable
issuers are applied. A significant increase in credit risk could result in a lower
fair value, whereas a significant decrease could result in a higher fair value. However,
a relative change of 10% in the credit spread does not materially affect the fair
value. Embedded derivatives are separated from their respective host contracts. Such host
contracts are generally sale or purchase agreements relating to the operational business.
The embedded derivatives cause the cash flows from the contracts to vary with exchange-rate
or price fluctuations. The internal measurement of embedded derivatives is mainly
performed using the discounted cash flow method, which is based on unobservable inputs.
These include planned sales and purchase volumes, and prices derived from market data.
Regular monitoring is carried out based on these fair values as part of quarterly
reporting. Within the financial liabilities, use was made of the fair value option according
to IAS 39.11A for the debt instruments (exchangeable bond) issued in June 2017 that
can be converted into Covestro shares. This exchangeable bond is a hybrid financial
instrument containing a debt instrument as a nonderivative host contract and several
embedded derivatives. Due to the application of the fair value option, the bond was
designated as a financial liability at fair value through profit or loss at its initial
recognition including the embedded derivatives. The changes in the amounts of financial assets and liabilities recognized at fair
value based on unobservable inputs (Level 3) for each financial instrument category
were as follows: B 21Development of Financial Assets and Liabilities (Level 3)
B 22Development of Financial Assets and Liabilities (Level 3)
The changes recognized in profit or loss were included in other operating income /
expenses, interest income or exchange gains / losses. Interest held in Covestro reduced to 40.9%In the first quarter, Bayer sold 22 million shares of Covestro AG to institutional
investors at a price of €66.50 per share. In the second quarter, Bayer sold a further
17.25 million shares of Covestro AG to institutional investors at a price of €62.25
per share. In addition, 8 million shares of Covestro AG were deposited in Bayer Pension
Trust e. V. at a price of €63.04, thus reducing the pension provisions of Bayer AG
by €504 million. The transactions had a €3.0 billion positive effect on Bayer Group equity, with €2.0
billion attributable to shareholders of Bayer AG and €1.0 billion to noncontolling
interest. Bayer reduced its interest in Covestro AG from 64.2% to 40.9% of the issued
shares. Legal risksTo find out more about the Bayer Group's legal risks, please see Note 32 to the consolidated
financial statements in the Bayer Annual Report 2016, which can be downloaded free
of charge at www.bayer.com. Since the Bayer Annual Report 2016, the following significant
changes have occurred in respect of the legal risks: Mirena™: As of July 13, 2017, lawsuits from approximately 3,000 users of Mirena™, an intrauterine system providing long-term contraception, had been served upon Bayer in the United States. Plaintiffs allege personal injuries resulting from the use of Mirena™, including perforation of the uterus, ectopic pregnancy or idiopathic intracranial hypertension, and seek compensatory and punitive damages. Additional lawsuits are anticipated. In April 2017, most of the cases pending in U.S. federal courts in which plaintiffs allege idiopathic intracranial hypertension were consolidated in a second multidistrict litigation proceeding for common pre-trial management. The first multidistrict litigation proceeding concerns perforation cases. Xarelto™: As of July 13, 2017, U.S. lawsuits from approximately 19,900 recipients of Xarelto™, an oral anticoagulant for the treatment and prevention of blood clots, had been served upon Bayer. Plaintiffs allege that users have suffered personal injuries from the use of Xarelto™, including cerebral, gastrointestinal or other bleeding and death, and seek compensatory and punitive damages. Additional lawsuits are anticipated. In May and June 2017, the first two cases set for trial in the federal multidistrict litigation resulted in complete defense verdicts. Two further trials have been scheduled this year (one in the federal multi district litigation, one in the Pennsylvania state court). Bayer anticipates that additional trials will be scheduled. As of July 13, 2017, ten Canadian lawsuits relating to Xarelto™ seeking class action certification had been served upon Bayer. Essure™: As of July 13, 2017, U.S. lawsuits from approximately 5,700 users of Essure™, a medical device offering permanent birth control with a nonsurgical procedure, had been served upon Bayer. Plaintiffs allege personal injuries from the use of Essure™, including hysterectomy, perforation, pain, bleeding, weight gain, nickel sensitivity, depression and unwanted pregnancy, and seek compensatory and punitive damages. Additional lawsuits are anticipated. As of July 13, 2017, two Canadian lawsuits relating to Essure™ seeking class action certification had been served upon Bayer. Related partiesRelated parties as defined in IAS 24 (Related Party Disclosures) are those legal entities
and natural persons that are able to exert influence on Bayer AG and its subsidiaries
or over which Bayer AG or its subsidiaries exercise control or joint control or have
a significant influence. They include, in particular, nonconsolidated subsidiaries,
joint ventures and associates included in the consolidated financial statements at
cost of acquisition or using the equity method, post-employment benefit plans and
the corporate officers of Bayer AG. In the second quarter, Bayer AG increased the coverage of Bayer Pension Trust e.V.
with the deposit of 8 million of the shares it held in Covestro AG. The number of
shares deposited amounted to 4.0% of the issued shares of Covestro AG and had a value
of €504 million. Sales to related parties were not material from the viewpoint of the Bayer Group.
Goods and services in the amount of €0.3 billion were procured from the associate
PO JV, LP, Wilmington, United States, mainly in the course of day-to-day business
operations. There was no significant change in receivables vis-à-vis related parties
compared with December 31, 2016. Liabilities declined by €0.1 billion to €0.2 billion,
with the greater part of the decrease pertaining to Casebia Therapeutics Limited Liability
Partnership, Ascot, United Kingdom, the newly established joint venture with CRISPR
Therapeutics AG, Basel, Switzerland. Other informationThe Annual Stockholders' Meeting on April 28, 2017, approved the proposal by the Board
of Management and the Supervisory Board that a dividend of €2.70 per share be paid
for the 2016 fiscal year. The actions of the members of the Board of Management and the Supervisory Board in
office in 2016 were ratified in accordance with the proposals by the Board of Management
and the Supervisory Board. Six stockholder representatives were elected to the Supervisory Board in accordance
with the nominations submitted by the Supervisory Board. Furthermore, in accordance with the proposal by the Board of Management and the Supervisory
Board, the Annual Stockholders' Meeting approved the amendment to the Articles of
Incorporation with regard to the compensation of the members of the Supervisory Board. The Annual Stockholders' Meeting also approved the control agreement between Bayer
AG and Bayer CropScience Aktiengesellschaft of February 21, 2017, as proposed by the
Board of Management and the Supervisory Board. In accordance with the proposal by the Supervisory Board, Deloitte GmbH Wirtschaftsprüfungsgesellschaft,
Munich, was elected as the auditor of the annual and consolidated financial statements
for the fiscal year 2017 and to review the condensed financial statements and interim
management reports as of June 30, 2017, September 30, 2017 and March 31, 2018. Leverkusen, July 25, 2017 Bayer Aktiengesellschaft The Board of Management
Responsibility StatementTo the best of our knowledge, and in accordance with the applicable reporting principles
for interim financial reporting, the interim consolidated financial statements give
a true and fair view of the assets, liabilities, financial position and profit or
loss of the Bayer Group, and the interim management report includes a fair review
of the development and performance of the business and the position of the Bayer Group,
together with a description of the principal opportunities and risks associated with
the expected development of the Bayer Group for the remaining months of the financial
year. Leverkusen, July 25, 2017 Bayer Aktiengesellschaft The Board of Management
Review ReportTo Bayer Aktiengesellschaft, Leverkusen, Germany We have reviewed the condensed interim consolidated financial statements - comprising
the income statement and the statement of comprehensive income, the statement of financial
position, the statement of cash flows, the condensed statement of changes in equity
as well as selected explanatory notes to the financial statements - and the interim
group management report for the period from 1 January 2017 until 30 June 2017 of Bayer
AG, which are components of the half-year financial report under § 37w WpHG (Wertpapierhandelsgesetz:
German Securities Trading Act). Review Report on the Condensed Interim Consolidated Financial StatementsManagement Board's Responsibility for the Condensed Interim Consolidated Financial StatementsThe preparation of the condensed interim consolidated financial statements in accordance
with the IFRS applicable to interim financial reporting as adopted by the EU is the
responsibility of the entity's Management Board. The Management Board is also responsible
for such internal control as the Management Board determines is necessary to enable
the preparation of condensed interim consolidated financial statements that are free
from material misstatement, whether due to fraud or error. Practitioner's Responsibility for the Review of the Condensed Interim Consolidated Financial StatementsOur responsibility is to express a conclusion on the condensed interim consolidated
financial statements based on our review. We conducted our review in accordance with
the German generally accepted standards for the review of financial statements promulgated
by the Institut der Wirtschaftsprüfer (IDW) as well as in supplementary compliance
with the International Standard on Review Engagements "Engagements to Review Historical
Financial Statements" (ISRE 2400 (revised)). Those standards require that we plan
and perform the review in compliance with professional standards such that we can
preclude through critical evaluation, with limited assurance, that the condensed interim
consolidated financial statements have not been prepared, in all material respects,
in accordance with the IFRS applicable to interim financial reporting as adopted by
the EU. A review of the condensed interim consolidated financial statements in accordance
with the German generally accepted standards for the review of financial statements
promulgated by the Institut der Wirtschaftsprüfer (IDW) as well as in supplementary
compliance with ISRE 2400 (revised) is a limited assurance engagement. A review is
limited primarily to inquiries of personnel of the entity and analytical procedures
and therefore does not provide the assurance attainable in a financial statement audit.
Since, in accordance with our engagement, we have not performed a financial statement
audit, we cannot issue an auditor's report. Conclusion on the Condensed Interim Consolidated Financial StatementsBased on our review, no matters have come to our attention that cause us to presume
that the condensed interim consolidated financial statements have not been prepared,
in all material respects, in accordance with the IFRS applicable to interim financial
reporting as adopted by the EU. Other Legal and Regulatory RequirementsReview Report on the Interim Group Management ReportManagement Board's Responsibility for the Interim Group Management ReportThe preparation of the interim group management report in accordance with the requirements
of the WpHG applicable to interim group management reports is the responsibility of
the entity's Management Board. The Management Board is also responsible for such internal
control as the Management Board determines is necessary to enable the preparation
of an interim group management report that is free from material misstatement, whether
due to fraud or error. Practitioner's Responsibility for the Review of the Interim Group Management ReportOur responsibility is to express a conclusion on the interim group management report
based on our review. We conducted our review in accordance with the German generally
accepted standards for the review of financial statements promulgated by the Institut
der Wirtschaftsprüfer (IDW) as well as in supplementary compliance with the International
Standard on Review Engagements "Engagements to Review Historical Financial Statements"
(ISRE 2400 (revised)). Those standards require that we plan and perform the review
in compliance with professional standards such that we can preclude through critical
evaluation, with limited assurance, that the interim group management report has not
been prepared, in all material respects, in accordance with the requirements of the
WpHG applicable to interim group management reports. A review of the interim group management report in accordance with the German generally
accepted standards for the review of financial statements promulgated by the Institut
der Wirtschaftsprüfer (IDW) as well as in supplementary compliance with ISRE 2400
(revised) is a limited assurance engagement. A review is limited primarily to inquiries
of personnel of the entity and analytical procedures and therefore does not provide
the assurance attainable in a financial statement audit. Since, in accordance with
our engagement, we have not performed a financial statement audit, we cannot issue
an auditor's report. Conclusion on the Interim Group Management ReportBased on our review, no matters have come to our attention that cause us to presume
that the interim group management report has not been prepared, in all material respects,
in accordance with the requirements of the WpHG applicable to interim group management
reports. Munich, Germany, 26 July 2017 Deloitte GmbH Wirtschaftsprüfungsgesellschaft
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